Canonical Allele Identifier: CA2486313671
Gene: PTPN14 HGNC NCBI

Linked Data

dbSNP Id: rs17042140

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214501582T>A , CM000663.2:g.214501582T>A GRCh38
NC_000001.10:g.214674925T>A , CM000663.1:g.214674925T>A GRCh37
NC_000001.9:g.212741548T>A NCBI36
NG_028036.1:g.55100A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000366956.10:c.-154-36625A>T MANE Select ENSP00000355923.4:n.-154-36625A>T
ENST00000366956.9:c.-154-36625A>T ENSP00000355923.4:n.-154-36625A>T
ENST00000486173.1:n.232-36625A>T
ENST00000543945.5:c.-154-36625A>T ENSP00000443330.1:n.-154-36625A>T
NM_005401.4:c.-154-36625A>T NP_005392.2:n.-154-36625A>T
XR_247032.3:n.421-36625A>T
XM_017001941.1:c.-155+31735A>T XP_016857430.1:n.-155+31735A>T
XM_024448759.1:c.-155+30882A>T XP_024304527.1:n.-155+30882A>T
NM_005401.5:c.-154-36625A>T MANE Select NP_005392.2:n.-154-36625A>T